Cystic Fibrosis in Children

Cystic fibrosis (CF) is an inherited genetic disorder that affects the lungs and digestive system. It causes thick, sticky mucus to build up in these organs, leading to breathing difficulties, frequent infections, and problems with digestion. Children with CF may experience persistent cough, wheezing, poor growth, and difficulty gaining weight. Since it’s a chronic condition, they require ongoing treatment with medications, airway clearance therapies, and nutritional support. Advances in care have improved life expectancy, but CF remains a serious condition that requires comprehensive management to help children lead healthier lives.